Regulatory Specialist - Cri

Methodist Health System•Dallas, TX

12d•Onsite

About The Position

The Regulatory Specialist will perform expertise in the regulatory component of all clinical research trials to include, but not limited to; Phase II and IV clinical, investigator initiated trials (IITs), and retrospective analysis of clinical data. The Regulatory Specialist will support the mission, vision, values, and strategies of the Methodist Health System.

Requirements

Bachelor's degree required
1 year of experience in a medical or clinical setting (required)
1 year of experience in clinical research (required)
1 year of experience in research regulatory affairs (required)
Strong proficiency using Microsoft Office products
Superior oral and written communication skills
Strong process orientation
Detail oriented, logical, and methodological approach to problem solving
Ability to provide vision and leadership.

Nice To Haves

Master’s degree preferred
CCRC or CCRP (preferred)
GCP certification (preferred)

Responsibilities

Communicate clearly and openly
Build relationships to promote a collaborative environment
Be accountable for your performance
Always look for ways to improve the patient experience
Take initiative for your professional growth
Be engaged and eager to build a winning team
Review clinical research protocols to determine logistical components of regulatory requirements
Obtain and facilitate tracking of relevant regulatory documents for clinical trials submission and management.
Maintain appropriate communications between sponsors, investigators, other research team members for clinical trials assigned.
Assist in the development of clinical trial documents for signature of principal investigator and approval by the IRB.
Create and/or adapt clinical trial informed consent documents for Institutional Review Board (IRB) submission.
Maintain regulatory documents in accordance with International Conference on Harmonization (ICH) and Good Clinical Practice (GCP) guidelines.
Attend study specific training, investigator meetings as assigned, and MHS required training.
Facilitate informed consent process for principal and sub-investigators.
Assist clinical research coordinators in the identification and reporting of appropriate adverse events in accordance with Food and Drug Administration, sponsor protocol, and IRB regulations and guidelines.
Prepare and submit amendments to protocols and informed consent documents as required.